| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218708 | Tetrahedron | 2012 | 4 Pages |
Abstract
A novel and convenient synthesis of 2,5,7-trisubstituted oxazolo[5,4-d]pyrimidines was presented. The key step involved an intramolecular C-O cross-coupling of the ortho-halopyrimidine amide via a copper (I)-mediated cyclization reaction, which provided target trisubstituted oxazolopyrimidine in moderate to good yields.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Dan Xu, Li-Ping Sun, Qi-Dong You,
![First Page Preview: Facile synthesis of 2,5,7-trisubstituted oxazolo[5,4-d]pyrimidines via copper-catalyzed intramolecular C-O bond formation Facile synthesis of 2,5,7-trisubstituted oxazolo[5,4-d]pyrimidines via copper-catalyzed intramolecular C-O bond formation](/preview/png/5218708.png)